Mutations in GATA2 are associated with the autosomal dominant and sporadic monocytopenia and mycobacterial infection (MonoMAC) syndrome

Lignende værker

• GATA2 haploinsufficiency caused by mutations in a conserved intronic element leads to MonoMAC syndrome
  af: Hsu, Amy P., et al.
  Udgivet: (2013)
• Autosomal dominant and sporadic monocytopenia with susceptibility to mycobacteria, fungi, papillomaviruses, and myelodysplasia
  af: Vinh, Donald C., et al.
  Udgivet: (2010)
• MonoMAC Syndrome in a Patient With a GATA2 Mutation: Case Report and Review of the Literature
  af: Camargo, Jose F., et al.
  Udgivet: (2013)
• Myelodysplasia in autosomal dominant and sporadic monocytopenia immunodeficiency syndrome: diagnostic features and clinical implications
  af: Calvo, Katherine R., et al.
  Udgivet: (2011)
• Mutational profiling of a MonoMAC syndrome family with GATA2 deficiency
  af: Ding, Ling-Wen, et al.
  Udgivet: (2016)